Canonical Allele Identifier: CA1310508294

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178527610C= , CM000664.2:g.178527610C=	GRCh38
NC_000002.11:g.179392337C= , CM000664.1:g.179392337C=	GRCh37
NC_000002.10:g.179100583C=	NCBI36
NG_011618.3:g.308193G= , LRG_391:g.308193G=
NG_051363.1:g.9784C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.99812G= (TTN)	ENSP00000343764.6:p.Ser33271=
ENST00000342175.11:c.80897G= (TTN)	ENSP00000340554.6:p.Ser26966=
ENST00000359218.10:c.80696G= (TTN)	ENSP00000352154.5:p.Ser26899=
ENST00000342175.10:c.80897G= (TTN)	ENSP00000340554.6:p.Ser26966=
ENST00000342992.10:c.99812G= (TTN)	ENSP00000343764.6:p.Ser33271=
ENST00000359218.9:c.80696G= (TTN)	ENSP00000352154.5:p.Ser26899=
ENST00000460472.6:c.80321G= (TTN)	ENSP00000434586.1:p.Ser26774=
ENST00000589042.5:c.107516G= (TTN) MANE Select	ENSP00000467141.1:p.Ser35839=
ENST00000591111.5:c.102593G= (TTN)	ENSP00000465570.1:p.Ser34198=
ENST00000615779.4:c.102593G= (TTN)	ENSP00000483597.1:p.Ser34198=
NM_001256850.1:c.102593G= (TTN)	NP_001243779.1:p.Ser34198=
NM_001267550.2:c.107516G= (TTN) MANE Select	NP_001254479.2:p.Ser35839=
NM_003319.4:c.80321G= (TTN)	NP_003310.4:p.Ser26774=
NM_133378.4:c.99812G= (TTN)	NP_596869.4:p.Ser33271=
NM_133432.3:c.80696G= (TTN)	NP_597676.3:p.Ser26899=
NM_133437.4:c.80897G= (TTN)	NP_597681.4:p.Ser26966=
NR_038271.1:n.446+3974C= (TTN-AS1)
NR_038272.1:n.219+3974C= (TTN-AS1)
XM_011511729.1:c.106613G= (TTN)	XP_011510031.1:p.Ser35538=
XM_011511730.1:c.80507G= (TTN)	XP_011510032.1:p.Ser26836=
XM_011511731.1:c.80366G= (TTN)	XP_011510033.1:p.Ser26789=
XM_017004819.1:c.106409G= (TTN)	XP_016860308.1:p.Ser35470=
XM_017004820.1:c.101807G= (TTN)	XP_016860309.1:p.Ser33936=
XM_017004821.1:c.101804G= (TTN)	XP_016860310.1:p.Ser33935=
XM_017004822.1:c.98846G= (TTN)	XP_016860311.1:p.Ser32949=
XM_017004823.1:c.80462G= (TTN)	XP_016860312.1:p.Ser26821=
XM_024453094.1:c.101957G= (TTN)	XP_024308862.1:p.Ser33986=
XM_024453095.1:c.101954G= (TTN)	XP_024308863.1:p.Ser33985=
XM_024453096.1:c.101387G= (TTN)	XP_024308864.1:p.Ser33796=
XM_024453097.1:c.98729G= (TTN)	XP_024308865.1:p.Ser32910=
XM_024453098.1:c.98648G= (TTN)	XP_024308866.1:p.Ser32883=
XM_024453099.1:c.80411G= (TTN)	XP_024308867.1:p.Ser26804=
XM_024453100.1:c.70265G= (TTN)	XP_024308868.1:p.Ser23422=